Mutation Analysis of 17α-Hydroxylase

NCT00172510 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2005-09-15

No results posted yet for this study

Summary

To elucidate the molecular pathology of the 4 families with 17α-hydroxylase/17,20-lyase deficiency.

Conditions

  • Pseudohermaphroditism
  • Congenital Adrenal Hyperplasia
  • Hypertension

Interventions

PROCEDURE

blood drawing

Sponsors & Collaborators

  • National Taiwan University Hospital

    lead OTHER

Principal Investigators

  • Yi-Ching Tung, MD · National Taiwan University Hospital

Eligibility

Min Age
0 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-08-31
Completion
2005-08-31

Countries

  • Taiwan

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00172510 on ClinicalTrials.gov